x

Cerca un test diagnostico

* (*) campo obbligatorio

MVZ wagnerstibbe fr Laboratoriumsmedizin, Hmostaseologie, Humangenetik und Mikrobiologie

  • amedes genetics im MVZ wagnerstibbe
  • Georgstr. 50
  • 30159 HANNOVER
  • GERMANIA
  • Stato : Public
  • Telefono : 49 (0)511 301795 0
  • Altro telefono : -
  • Fax : 49 (0)511 301795 119
  • Sito web
  • email di contatto
  • Numero EUGT : EUGTDE50360

Contatti

Gestione della qualit

Accreditato							
 Accreditamento

Accreditamento
Ente
Anno
Ambito dellaccreditamento

VEQ VEQ

VEQ elencate per CF Network

CF (Cystic fibrosis)
2017, 2018, 2019

VEQ elencate per EMQN

AZF (Y-Chromosome microdeletions)
2016, 2017, 2018, 2019
BRAF (Molecular testing for malignant melanoma)
2019
CMT/HNPP (Charcot-Marie-Tooth disease / Hereditary Neuropathy with Pressure Palsies)
2016, 2017, 2018, 2019
Cardiac genetics - Hypertrophic cardiomyopathies
2018, 2019
Cardiac genetics - arrthymias
2018, 2019
DFNB1 (Hereditary Deafness)
2016, 2017, 2018, 2019
DMD (Duchenne and Becker muscular dystrophies)
2019
EGFR (Molecular testing for non small cell lung cancer)
2016, 2017, 2018, 2019
FAP (Familial Adenomatous Polyposis Colon Cancer)
2019
FH (Familial hypercholesterolemia - pilot scheme)
2016, 2017, 2018, 2019
FRAX (Fragile X syndrome) - full scheme
2018, 2019
Germline NGS mutation testing
2016, 2017, 2018, 2019
HBOC (Hereditary Breast and Ovarian Cancer testing)
2016, 2017, 2018, 2019
HD (Huntington disease)
2019
HFE (Hereditary hemochromatosis)
2018
HNPCC (Hereditary non-polyposis colon cancer)
2016, 2017, 2018, 2019
HRF (Hereditary Recurrent Fevers)
2016, 2017, 2018, 2019
KRAS (Molecular testing for sporadic colorectal cancer)
2017, 2018, 2019
MEN2 (Multiple Endocrine Neoplasia Type 2)
2016, 2017, 2018, 2019
Molecular testing of germline changes in BRCA genes for ovarian cancer
2017, 2018, 2019
Molecular testing of somatic changes in BRCA genes for ovarian cancer
2017, 2018, 2019
MonoDiab (Monogenic Diabetes)
2016, 2017, 2018, 2019
Non-invasive prenatal testing (NIPT) for common aneuploidies
2018, 2019
Non-invasive prenatal testing (NIPT) for fetal sexing
2018
OI (Osteogenesis imperfecta)
2016, 2017, 2018, 2019
ONCOPANEL (Oncogene panel testing) - pilot scheme
2017, 2018
PWAS (Prader-Willi and Angelman syndromes)
2016, 2017, 2018, 2019
RYR1 related disorders
2019
SEQ (DNA sequencing) - Full scheme
2017, 2018, 2019
SHOX (Short stature homeobox gene testing)
2016, 2017, 2018, 2019
SMA (Spinal muscular atrophy)
2017, 2018, 2019
Somatic NGS mutation testing
2019
Stickler syndrome
2019
VHL (Von Hippel Lindau syndrome)
2016, 2017, 2018, 2019
WIL (Wilson disease)
2018, 2019
aCGH/ Microarrays
2016, 2017
Tutte le informazioni presenti nel sito non sostituiscono in alcun modo il giudizio di un medico specialista, l'unico autorizzato ad effettuare una consulenza medica ed esprimere un parere medico.